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The Journal of Neurophysiology Vol. 82 No. 4 October 1999, pp. 1865-1875
Copyright ©1999 by the American Physiological Society
1Cerebral and Sensory Functions Unit,
Wilson, P.,
P. D. Kitchener, and
P. J. Snow.
Cutaneous Receptive Field Organization in the Ventral Posterior
Nucleus of the Thalamus in the Common Marmoset. J. Neurophysiol. 82: 1865-1875, 1999. The organization of
cutaneous receptive fields in the ventroposterior (VP) thalamus of the
common marmosets (Callithrix jacchus) was determined
from single-unit recordings, and these data were correlated with the
cytochrome oxidase (CO) histochemistry of the thalamus in the same
animals. Under continuously maintained ketamine anesthesia, the
receptive fields of a total of 192 single units were recorded from the
right VP thalamus using 2 M
glass microelectrodes. After the
receptive fields were mapped, the brains were reacted for CO
histochemistry on 50-µm coronal frozen sections through the entire VP
thalamus. The majority of units were localized to the CO-reactive
regions that define the medial and lateral divisions of VP (VPm and
VPl). Apart from the expected finding of the face being represented in
VPm and the body in VPl, reconstructing the electrode tracks and unit
locations in the histological sections revealed a general association
between discrete regions of CO reactivity and the representation of
specific body regions. Some low-threshold cutaneous units were
apparently localized to VPi (the CO weak regions dorsal, ventral, and
interdigitating with, the CO regions of VP). These VPi units were
clearly part of the same representational map as the VPl and VPm units.
We conclude that the low-threshold cutaneous receptive fields of the
marmoset are organized in a single continuous representation of the
contralateral body surface, and that this representation can most
simply be interpreted as being folded or crumpled into the
three-dimensional space of VP thalamus. The folded nature of the body
map in VP may be related to the folded nature of VP as revealed by CO histochemistry.
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